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CDw17 antibody

This Mouse Monoclonal antibody specifically detects CDw17 in FACS and IF. It exhibits reactivity toward Human.
Catalog No. ABIN6941312
-15% Promotion 2026
$544.39
$640.46
save $96.07 (-15 %)
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Quick Overview for CDw17 antibody (ABIN6941312)

Target

CDw17

Reactivity

Human

Host

  • 4
Mouse

Clonality

  • 4
Monoclonal

Conjugate

  • 4
Un-conjugated

Application

  • 4
  • 4
  • 1
  • 1
Flow Cytometry (FACS), Immunofluorescence (IF)

Clone

HuLy-m13
  • Immunogen

    β-2 Microglobulin associated proteins from a detergent lysate of human PBL

    Isotype

    IgM kappa
  • Application Notes

    Positive Control: Human PBL. Tonsil.

    Known Application: Flow Cytometry (0.5-1 μg/million cells), Immunofluorescence (0.5-1 μg/mL), Optimal dilution for a specific application should be determined.

    Restrictions

    For Research Use only
  • Concentration

    200 μg/mL

    Buffer

    10 mM PBS with 0.05 % BSA & 0.05 % azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-80 °C

    Storage Comment

    Antibody with azide - store at 2 to 8°C. Antibody without azide - store at -20 to -80°C. Antibody is stable for 24 months. Non-hazardous. No MSDS required.

    Expiry Date

    24 months
  • Target

    CDw17

    Background

    CD17 is an intermediate glycosphingolipid from the metabolism of higher gangliosides that localizes to sphingolipid-sterol rafts. CD17 is detectable in monocytes, granulocytes, basophils, platelets, a subset of peripheral B cells (CD19+) and tonsil dendritic cells. It is rapidly down regulated on activated granulocytes and is upregulated on IL-2 activated T lymphocytes. CD17 binds to bacteria and may function in phagocytosis. VEGF-treated endothelial cells can produce CD17, which can then mediate signaling toward PECAM-1 expression and angiogenesis. Tumor necrosis factor )-induced astrogliosis (astrocyte proliferation and glial fibrillary acidic protein (GFAP) upregulation) in response to neuro-inflammation (i.e. spinal cord injury) causes an increase in intracellular levels of CD17. Aberrant levels of glycosphingolipids are a feature of cancer cells and may influence integrin clustering and internalization.
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